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Exosome Therapy for Male Androgenetic Alopecia

6. juli 2026 opdateret af: Zhang Han

A Randomized, Double-Blind, Placebo-Controlled Clinical Trial Evaluating the Efficacy and Safety of Human Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes for the Treatment of Male Androgenetic Alopecia

The goal of this clinical trial is to learn if local scalp injection of human umbilical cord mesenchymal stem cell-derived exosomes (hUCMSC-Exos) can treat androgenetic alopecia (AGA) in male patients with AGA.

The main question it aims to answer is:

Does hUCMSC-Exos injection improve hair regrowth compared with placebo?

Researchers will compare hUCMSC-Exos injection to placebo injection to see if hUCMSC-Exos leads to superior efficacy in hair follicle regeneration, as measured by changes in hair density, hair thickness, and patient-reported outcomes.

Participants will:

Receive randomized, double-blinded local scalp injections of either hUCMSC-Exos or placebo

Attend scheduled follow-up visits for hair assessment and safety monitoring

Undergo photography, trichoscopy, and complete quality-of-life or psychosocial burden questionnaires as applicable

Studieoversigt

Detaljeret beskrivelse

Androgenetic alopecia (AGA) is a chronic, progressive condition characterized by gradual miniaturization of hair follicles in a patterned distribution, primarily influenced by genetic susceptibility and androgen-mediated signaling pathways. The condition involves disruption of the hair cycle, particularly shortening of the anagen phase and progressive conversion of terminal hair follicles into vellus-like follicles, ultimately resulting in visible hair thinning and reduced hair density. In addition to its dermatological manifestations, AGA is associated with significant psychological burden, including decreased self-confidence and impaired quality of life.

Current pharmacological interventions mainly aim to slow disease progression rather than fully restore follicular function. However, their limited efficacy and dependency on continuous administration highlight the unmet need for regenerative and disease-modifying therapeutic strategies.

Mesenchymal stem cell-derived exosomes (MSC-Exos) represent a novel class of cell-free biologics with regenerative and immunomodulatory properties. These nano-sized extracellular vesicles contain bioactive molecules such as proteins, lipids, and nucleic acids, which mediate intercellular communication and regulate multiple biological processes. Among different MSC sources, human umbilical cord-derived MSCs are considered to possess advantageous biological characteristics, including higher proliferative capacity, lower immunogenicity, and more stable paracrine activity, making their exosomes particularly suitable for clinical translation.

Experimental studies have demonstrated that MSC-Exos may influence hair follicle biology through multiple complementary mechanisms, including modulation of dermal papilla cell activity, regulation of signaling pathways involved in follicular cycling, enhancement of vascular support within the perifollicular environment, and attenuation of local inflammatory responses. These combined effects may contribute to the reactivation of dormant follicles and support the transition of hair follicles into the anagen growth phase.

This clinical investigation is designed to translate these preclinical findings into a controlled human study setting, aiming to systematically evaluate the therapeutic potential of hUCMSC-derived exosomes for hair regeneration. The study will generate evidence regarding both clinical efficacy and safety profile, providing foundational data for future development of exosome-based regenerative therapies in androgenetic alopecia.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

120

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

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Beskrivelse

Inclusion Criteria

Participants must meet all of the following criteria to be eligible for enrollment:

  1. Male subjects aged 18 to 55 years;
  2. Diagnosis of androgenetic alopecia classified as Norwood-Hamilton grade III-V;
  3. Stable pattern of hair loss for at least 6 months prior to screening;
  4. Willingness to refrain from using any other hair loss treatments during the study period and for 6 months after completion of treatment.

Exclusion Criteria

Participants meeting any of the following criteria will be excluded:

  1. Other types of alopecia, including alopecia areata, cicatricial alopecia, or telogen effluvium;
  2. Use of minoxidil, finasteride, spironolactone, or other hair growth-related medications within 1 year prior to screening;
  3. Receipt of platelet-rich plasma (PRP), laser cap therapy, or other scalp procedures within 6 months prior to screening;
  4. History of autoimmune disease, active scalp infection, coagulation disorders, or malignancy;
  5. Known hypersensitivity to the investigational product or any of its components;
  6. Inability to comply with study procedures, incomplete clinical data, or conditions that may interfere with efficacy evaluation;
  7. Participation in another clinical trial within the study period;
  8. Any condition that, in the opinion of the investigator, makes the participant unsuitable for the study.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Normal saltvandsinjektion
Sterile 0.9% normal saline injection. Administered via intradermal scalp injection using the same protocol as the experimental group: 0.05 mL per point, 1 cm spacing, approximately 4 mm depth, once every 4 weeks for a total of 3 sessions.
Eksperimentel: hUCMSC-Exosome Injection
Sterile exosome suspension derived from human umbilical cord mesenchymal stem cells (hUCMSC-Exos). Administered via intradermal scalp injection at 0.05 mL per point, 1 cm spacing, approximately 4 mm depth. Treatment repeated once every 4 weeks for a total of 3 sessions.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Hair Density From Baseline to Week 24
Tidsramme: Baseline to Week 24
Hair density (hairs/cm²) within a predefined target scalp area will be assessed using digital trichoscopy.
Baseline to Week 24
Change in Modified Global Photographic Assessment (MGPA) Score From Baseline to Week 24
Tidsramme: Baseline to Week 24
Global scalp photographs will be evaluated by blinded investigators using the Modified Global Photographic Assessment (MGPA) scale to assess overall improvement in hair growth.
Baseline to Week 24

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Change in Hair Density From Baseline to Week 12
Tidsramme: Baseline to Week 12
Hair density changes within the predefined target area measured by digital trichoscopy.
Baseline to Week 12
Change in Modified Global Photographic Assessment (MGPA) Score From Baseline to Week 12
Tidsramme: Baseline to Week 12
Assessment of global hair growth improvement using standardized photography and MGPA scoring.
Baseline to Week 12
Change in Dermatology Life Quality Index (DLQI) Score From Baseline to Week 24
Tidsramme: Baseline to Week 24
Evaluation of treatment-related quality of life improvement using the Dermatology Life Quality Index questionnaire.
Baseline to Week 24
Change in Mean Hair Shaft Diameter From Baseline to Week 24
Tidsramme: Baseline to Week 24
Mean hair shaft diameter will be measured using digital trichoscopic analysis.
Baseline to Week 24
Change in Hair Type Proportions From Baseline to Week 24
Tidsramme: Baseline to Week 24
Percentage changes in vellus hairs, intermediate hairs, and terminal hairs within the target scalp area.
Baseline to Week 24
Subject Satisfaction Score at Week 24
Tidsramme: Week 24
Participant-reported satisfaction regarding overall hair growth improvement and treatment outcomes.
Week 24
Investigator Satisfaction Assessment at Week 24
Tidsramme: Week 24
Overall investigator-rated assessment of treatment response and cosmetic improvement.
Week 24

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

30. april 2026

Primær færdiggørelse (Anslået)

10. november 2026

Studieafslutning (Anslået)

10. november 2026

Datoer for studieregistrering

Først indsendt

6. juli 2026

Først indsendt, der opfyldte QC-kriterier

6. juli 2026

Først opslået (Faktiske)

9. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

9. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

6. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

UBESLUTET

IPD-planbeskrivelse

Individual participant data (IPD) sharing has not yet been determined. Data sharing policies will be considered after study completion in accordance with institutional regulations, ethical requirements, and participant privacy protection.

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Kliniske forsøg med Androgenetisk alopeci (AGA)

3
Abonner